English  |  正體中文  |  简体中文  |  全文筆數/總筆數 : 12145/12927 (94%)
造訪人次 : 858801      線上人數 : 793
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
搜尋範圍 查詢小技巧：
  • 您可在西文檢索詞彙前後加上"雙引號"，以獲取較精準的檢索結果
  • 若欲以作者姓名搜尋，建議至進階搜尋限定作者欄位，可獲得較完整資料
    •  進階搜尋
    主頁 ‧ 登入 ‧ 上傳 ‧ 說明 ‧ 關於NHRI ‧ 管理 到手機版

    類別瀏覽

    正在載入社群分類, 請稍候....

    年代瀏覽

    正在載入年代分類, 請稍候....

    "Psaty, BM"的相關文件 

    回到依作者瀏覽

    顯示 15 項.

    類別 日期 題名 關聯 檔案
    [鍾仁華] 期刊論文 2020-09 Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale -
    [熊昭] 期刊論文 2020-10 Inherited causes of clonal haematopoiesis in 97,691 whole genomes -
    [鍾仁華] 期刊論文 2023-04-12 Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis -
    [鍾仁華] 期刊論文 2024-10-09 Rare variant contribution to the heritability of coronary artery disease -
    [鍾仁華] 期刊論文 2022-08-01 Insights from a large-scale whole-genome sequencing study of systolic blood pressure, diastolic blood pressure, and hypertension -
    [鍾仁華] 期刊論文 2022-10-11 Whole genome sequence analysis of blood lipid levels in >66,000 individuals -
    [許惠恒] 期刊論文 2023-06-29 Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study -
    [鍾仁華] 期刊論文 2023-12-14 Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores -
    [鍾仁華] 期刊論文 2024-05-30 Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores -
    [鍾仁華] 期刊論文 2021-03-11 Inherited causes of clonal haematopoiesis in 97,691 whole genomes[Erratum:Nature. 2020 Oct;586(7831):763-768.] -
    [鍾仁華] 期刊論文 2021-06-09 Variant-specific inflation factors for assessing population stratification at the phenotypic variance level -
    [張憶壽] 期刊論文 2022-10-27 A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies -
    [鍾仁華] 期刊論文 2022-12-23 Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies -
    [熊昭] 期刊論文 2023-02 Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing -
    [許惠恒] 期刊論文 2023-10-05 Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study -

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - 回饋